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      The enteric nervous system in gastrointestinal disease etiology

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          Abstract

          A highly conserved but convoluted network of neurons and glial cells, the enteric nervous system (ENS), is positioned along the wall of the gut to coordinate digestive processes and gastrointestinal homeostasis. Because ENS components are in charge of the autonomous regulation of gut function, it is inevitable that their dysfunction is central to the pathophysiology and symptom generation of gastrointestinal disease. While for neurodevelopmental disorders such as Hirschsprung, ENS pathogenesis appears to be clear-cut, the role for impaired ENS activity in the etiology of other gastrointestinal disorders is less established and is often deemed secondary to other insults like intestinal inflammation. However, mounting experimental evidence in recent years indicates that gastrointestinal homeostasis hinges on multifaceted connections between the ENS, and other cellular networks such as the intestinal epithelium, the immune system, and the intestinal microbiome. Derangement of these interactions could underlie gastrointestinal disease onset and elicit variable degrees of abnormal gut function, pinpointing, perhaps unexpectedly, the ENS as a diligent participant in idiopathic but also in inflammatory and cancerous diseases of the gut. In this review, we discuss the latest evidence on the role of the ENS in the pathogenesis of enteric neuropathies, disorders of gut–brain interaction, inflammatory bowel diseases, and colorectal cancer.

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          A genetic model for colorectal tumorigenesis.

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            Molecular Architecture of the Mouse Nervous System

            Summary The mammalian nervous system executes complex behaviors controlled by specialized, precisely positioned, and interacting cell types. Here, we used RNA sequencing of half a million single cells to create a detailed census of cell types in the mouse nervous system. We mapped cell types spatially and derived a hierarchical, data-driven taxonomy. Neurons were the most diverse and were grouped by developmental anatomical units and by the expression of neurotransmitters and neuropeptides. Neuronal diversity was driven by genes encoding cell identity, synaptic connectivity, neurotransmission, and membrane conductance. We discovered seven distinct, regionally restricted astrocyte types that obeyed developmental boundaries and correlated with the spatial distribution of key glutamate and glycine neurotransmitters. In contrast, oligodendrocytes showed a loss of regional identity followed by a secondary diversification. The resource presented here lays a solid foundation for understanding the molecular architecture of the mammalian nervous system and enables genetic manipulation of specific cell types.
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              Indigenous bacteria from the gut microbiota regulate host serotonin biosynthesis.

              The gastrointestinal (GI) tract contains much of the body's serotonin (5-hydroxytryptamine, 5-HT), but mechanisms controlling the metabolism of gut-derived 5-HT remain unclear. Here, we demonstrate that the microbiota plays a critical role in regulating host 5-HT. Indigenous spore-forming bacteria (Sp) from the mouse and human microbiota promote 5-HT biosynthesis from colonic enterochromaffin cells (ECs), which supply 5-HT to the mucosa, lumen, and circulating platelets. Importantly, microbiota-dependent effects on gut 5-HT significantly impact host physiology, modulating GI motility and platelet function. We identify select fecal metabolites that are increased by Sp and that elevate 5-HT in chromaffin cell cultures, suggesting direct metabolic signaling of gut microbes to ECs. Furthermore, elevating luminal concentrations of particular microbial metabolites increases colonic and blood 5-HT in germ-free mice. Altogether, these findings demonstrate that Sp are important modulators of host 5-HT and further highlight a key role for host-microbiota interactions in regulating fundamental 5-HT-related biological processes.
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                Author and article information

                Contributors
                werend.boesmans@uhasselt.be
                Journal
                Cell Mol Life Sci
                Cell Mol Life Sci
                Cellular and Molecular Life Sciences
                Springer International Publishing (Cham )
                1420-682X
                1420-9071
                26 March 2021
                26 March 2021
                2021
                : 78
                : 10
                : 4713-4733
                Affiliations
                [1 ]GRID grid.412966.e, ISNI 0000 0004 0480 1382, Department of Pathology, GROW-School for Oncology and Developmental Biology, , Maastricht University Medical Center, ; Maastricht, The Netherlands
                [2 ]GRID grid.12155.32, ISNI 0000 0001 0604 5662, Biomedical Research Institute (BIOMED), , Hasselt University, ; Diepenbeek, Belgium
                [3 ]GRID grid.412966.e, ISNI 0000 0004 0480 1382, Department of Internal Medicine, Division of Gastroenterology-Hepatology, NUTRIM-School of Nutrition and Translational Research in Metabolism, , Maastricht University Medical Center, ; Maastricht, The Netherlands
                [4 ]GRID grid.5645.2, ISNI 000000040459992X, Department of Clinical Genetics, , Erasmus MC University Medical Center, ; Rotterdam, The Netherlands
                Author information
                http://orcid.org/0000-0002-3150-4477
                http://orcid.org/0000-0001-7325-6021
                http://orcid.org/0000-0001-9856-9980
                http://orcid.org/0000-0002-9459-123X
                http://orcid.org/0000-0002-2426-0451
                Article
                3812
                10.1007/s00018-021-03812-y
                8195951
                33770200
                497c6d28-469b-4d87-a71a-aaf471e65924
                © The Author(s) 2021

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 20 November 2020
                : 20 February 2021
                : 10 March 2021
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100003130, Fonds Wetenschappelijk Onderzoek;
                Award ID: G036320N
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100001826, ZonMw;
                Award ID: VIDI: 016.196.367
                Award Recipient :
                Categories
                Review
                Custom metadata
                © Springer Nature Switzerland AG 2021

                Molecular biology
                neural crest,irritable bowel syndrome,inflammatory bowel disease,hirschsprung disease,microbiota

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